Canonical Allele Identifier: CA2680956618

Gene: SERAC1

Linked Data

• gnomAD v4: 6-158114706-C-CATTCAAGGAATATAAAATGAGATAATAA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114716_158114717insTATAAAATGAGATAATAAATTCAAGGAA , CM000668.2:g.158114716_158114717insTATAAAATGAGATAATAAATTCAAGGAA	GRCh38
NC_000006.11:g.158535748_158535749insTATAAAATGAGATAATAAATTCAAGGAA , CM000668.1:g.158535748_158535749insTATAAAATGAGATAATAAATTCAAGGAA	GRCh37
NC_000006.10:g.158455736_158455737insTATAAAATGAGATAATAAATTCAAGGAA	NCBI36
NG_032889.1:g.58574_58575insTTATTATCTCATTTTATATTCCTTGAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1404+82_*1404+83insTTATTATCTCATTTTATATTCCTTGAAT	ENSP00000475855.1:n.*1404+82_*1404+83insTTATTATCTCATTTTATATTC...
ENST00000642244.1:c.1594+82_1594+83insTTATTATCTCATTTTATATTCCTTGAAT	ENSP00000493554.1:n.1594+82_1594+83insTTATTATCTCATTTTATATTCCT...
ENST00000642903.1:c.*2_*3insTTATTATCTCATTTTATATTCCTTGAAT	ENSP00000493559.1:n.*2_*3insTTATTATCTCATTTTATATTCCTTGAAT
ENST00000644972.1:c.1684+82_1684+83insTTATTATCTCATTTTATATTCCTTGAAT	ENSP00000496451.1:n.1684+82_1684+83insTTATTATCTCATTTTATATTCCT...
ENST00000645077.1:c.*1305+82_*1305+83insTTATTATCTCATTTTATATTCCTTGAAT	ENSP00000496113.1:n.*1305+82_*1305+83insTTATTATCTCATTTTATATTC...
ENST00000645172.1:c.*1386+82_*1386+83insTTATTATCTCATTTTATATTCCTTGAAT	ENSP00000495367.1:n.*1386+82_*1386+83insTTATTATCTCATTTTATATTC...
ENST00000646190.1:n.3015+82_3015+83insTTATTATCTCATTTTATATTCCTTGAAT
ENST00000646208.1:c.1420+82_1420+83insTTATTATCTCATTTTATATTCCTTGAAT	ENSP00000493723.1:n.1420+82_1420+83insTTATTATCTCATTTTATATTCCT...
ENST00000646410.1:c.1555+82_1555+83insTTATTATCTCATTTTATATTCCTTGAAT	ENSP00000494205.1:n.1555+82_1555+83insTTATTATCTCATTTTATATTCCT...
ENST00000646562.1:c.*1600_*1601insTTATTATCTCATTTTATATTCCTTGAAT	ENSP00000496087.1:n.*1600_*1601insTTATTATCTCATTTTATATTCCTTGAA...
ENST00000647468.2:c.1684+82_1684+83insTTATTATCTCATTTTATATTCCTTGAAT MANE Select	ENSP00000496731.1:n.1684+82_1684+83insTTATTATCTCATTTTATATTCCT...
ENST00000648111.1:c.*1372+82_*1372+83insTTATTATCTCATTTTATATTCCTTGAAT	ENSP00000497275.1:n.*1372+82_*1372+83insTTATTATCTCATTTTATATTC...
ENST00000367104.7:c.1684+82_1684+83insTTATTATCTCATTTTATATTCCTTGAAT	ENSP00000356071.3:n.1684+82_1684+83insTTATTATCTCATTTTATATTCCT...
ENST00000435180.5:c.491_492insTTATTATCTCATTTTATATTCCTTGAAT	ENSP00000391168.1:n.491_492insTTATTATCTCATTTTATATTCCTTGAAT
ENST00000606965.5:c.*327_*328insTTATTATCTCATTTTATATTCCTTGAAT	ENSP00000475808.1:n.*327_*328insTTATTATCTCATTTTATATTCCTTGAAT
ENST00000607071.5:c.*1618+82_*1618+83insTTATTATCTCATTTTATATTCCTTGAAT	ENSP00000475855.1:n.*1618+82_*1618+83insTTATTATCTCATTTTATATTC...
ENST00000607742.5:c.*2962+82_*2962+83insTTATTATCTCATTTTATATTCCTTGAAT	ENSP00000475523.1:n.*2962+82_*2962+83insTTATTATCTCATTTTATATTC...
NM_032861.3:c.1684+82_1684+83insTTATTATCTCATTTTATATTCCTTGAAT	NP_116250.3:n.1684+82_1684+83insTTATTATCTCATTTTATATTCCTTGAAT
NR_073096.1:n.1699_1700insTTATTATCTCATTTTATATTCCTTGAAT
XM_006715586.1:c.1474+82_1474+83insTTATTATCTCATTTTATATTCCTTGAAT	XP_006715649.1:n.1474+82_1474+83insTTATTATCTCATTTTATATTCCTTGA...
XM_011536196.1:c.1663+82_1663+83insTTATTATCTCATTTTATATTCCTTGAAT	XP_011534498.1:n.1663+82_1663+83insTTATTATCTCATTTTATATTCCTTGA...
XM_011536197.1:c.1570+82_1570+83insTTATTATCTCATTTTATATTCCTTGAAT	XP_011534499.1:n.1570+82_1570+83insTTATTATCTCATTTTATATTCCTTGA...
XM_011536198.1:c.1474+82_1474+83insTTATTATCTCATTTTATATTCCTTGAAT	XP_011534500.1:n.1474+82_1474+83insTTATTATCTCATTTTATATTCCTTGA...
XM_006715586.3:c.1474+82_1474+83insTTATTATCTCATTTTATATTCCTTGAAT	XP_006715649.1:n.1474+82_1474+83insTTATTATCTCATTTTATATTCCTTGA...
XM_011536196.3:c.1663+82_1663+83insTTATTATCTCATTTTATATTCCTTGAAT	XP_011534498.1:n.1663+82_1663+83insTTATTATCTCATTTTATATTCCTTGA...
XM_011536198.3:c.1474+82_1474+83insTTATTATCTCATTTTATATTCCTTGAAT	XP_011534500.1:n.1474+82_1474+83insTTATTATCTCATTTTATATTCCTTGA...
XM_024446573.1:c.1684+82_1684+83insTTATTATCTCATTTTATATTCCTTGAAT	XP_024302341.1:n.1684+82_1684+83insTTATTATCTCATTTTATATTCCTTGA...
XR_001743697.2:n.1715+82_1715+83insTTATTATCTCATTTTATATTCCTTGAAT
XR_942606.2:n.1766+82_1766+83insTTATTATCTCATTTTATATTCCTTGAAT
NM_032861.4:c.1684+82_1684+83insTTATTATCTCATTTTATATTCCTTGAAT MANE Select	NP_116250.3:n.1684+82_1684+83insTTATTATCTCATTTTATATTCCTTGAAT
NR_073096.2:n.1681_1682insTTATTATCTCATTTTATATTCCTTGAAT